All diseases

OMIM ID
209920
OMIM term:
BARE LYMPHOCYTE SYNDROME, TYPE II
Alternative terms:
BLS, TYPE II
BARE LYMPHOCYTE SYNDROME; BLS
SEVERE COMBINED IMMUNODEFICIENCY, HLA CLASS II-NEGATIVE
SCID, HLA CLASS II-NEGATIVE BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP A, INCLUDED
BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP B, INCLUDED
BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP C, INCLUDED
BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP D, INCLUDED
BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP E, INCLUDED
(∗) Location:
13q13.3   16p13.13   19p13.11   1q21.3  
(†) Associated OMIM genes:
MHC2TA   RFX5   RFXANK   RFXAP  
(‡) Associated MGI genes:
Ciita  

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